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Upper Airway Cell Transcriptomics Identify a Major New Immunological Phenotype with Strong Clinical Correlates in Young Children with Acute Wheezing.

Reference
Khoo, Siew-Kim, Read, James, Franks, Kimberley, et al. Upper Airway Cell Transcriptomics Identify a Major New Immunological Phenotype with Strong Clinical Correlates in Young Children with Acute Wheezing. J Immunol. 2019;202(6):1845-1858. doi:10.4049/jimmunol.1800178
Abstract

Asthma exacerbations are triggered by rhinovirus infections. We employed a systems biology approach to delineate upper-airway gene network patterns underlying asthma exacerbation phenotypes in children. Cluster analysis unveiled distinct IRF7 versus IRF7 molecular phenotypes, the former exhibiting robust upregulation of Th1/type I IFN responses and the latter an alternative signature marked by upregulation of cytokine and growth factor signaling and downregulation of IFN-γ. The two phenotypes also produced distinct clinical phenotypes. For IRF7 children, symptom duration prior to hospital presentation was more than twice as long from initial symptoms ( = 0.011) and nearly three times as long for cough ( < 0.001), the odds ratio of admission to hospital was increased more than 4-fold ( = 0.018), and time to recurrence was shorter ( = 0.015). In summary, our findings demonstrate that asthma exacerbations in children can be divided into IRF7 versus IRF7 phenotypes with associated differences in clinical phenotypes.